Mitochondrial DNA Variation Dictates Expressivity and Progression of Nuclear DNA Mutations Causing Cardiomyopathy

Nuclear-encoded mutations causing metabolic and degenerative diseases have highly variable expressivity. Patients sharing the homozygous mutation (c.523delC) in the adenine nucleotide translocator 1 gene (SLC25A4, ANT1) develop cardiomyopathy that varies from slowly progressive to fulminant. This variability correlates with the mitochondrial DNA (mtDNA) lineage. To confirm that mtDNA variants can modulate the expressivity of nuclear DNA (nDNA)-encoded diseases, we combined in mice the nDNA Slc25a4−/− null mutation with a homoplasmic mtDNA ND6P25L or COIV421A variant. The ND6P25L variant significantly increased the severity of cardiomyopathy while the COIV421A variant was phenotypically neutral. The adverse Slc25a4−/− and ND6P25L combination was associated with impaired mitochondrial complex I activity, increased oxidative damage, decreased l-Opa1, altered mitochondrial morphology, sensitization of the mitochondrial permeability transition pore, augmented somatic mtDNA mutation levels, and shortened lifespan. The strikingly different phenotypic effects of these mild mtDNA variants demonstrate that mtDNA can be an important modulator of autosomal disease. [Display omitted] •Mitochondrial-nuclear interactions modulate autosomal mutation expressivity•mtDNA complex I and IV variants have opposing effects on Ant1−/− pathophysiology•Ant1−/− decreases OXPHOS complex I amount and complex V structural assembly•Somatic mtDNA mutations augment the effects of unfavorable mtDNA-nDNA interactions McManus et al. investigate mitochondrial-nuclear interactions in human disease by developing a murine model combining the Slc25a4 cardiomyopathy null gene mutation with mild mtDNA variants. Differences in mtDNA genotype can strongly influence autosomal gene mutations; conversely, accumulation of somatic mtDNA mutations can augment the deleterious consequences of mitochondrial-nuclear interactions.